Page 2520 - Williams Hematology ( PDFDrive )
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 2490  Index                                                                                            Index         2491



                     hemoglobin polymerization, 763–764  intermediate, 1353                Skeletal survey, in myeloma, 1715, 1748,
                     hemolysis and nitric oxide scavenging,   in megaloblastic anemia, 595        1748f
                         764                            morphology, 915–916                Skin disorders
                     inflammation and chronic vasculopathy,   normal, 465, 552, 623–624, 916f  in acute myelogenous leukemia, 1380,
                         765                            pathologic, 465, 466f, 916f               1410
                     ischemia–reperfusion injury, 765   ring, 178, 465, 567, 624, 918, 1353  in adult Langerhans cell histiocytosis, 1108
                    in pregnancy, 125–126             Siderocyte, 467f                      in antiphospholipid syndrome, 2240
                    transient aplastic crisis and, 541  Siderosomes, 465, 468               in chronic lymphocytic leukemia, 1541
                    treatment, 774–776                Siglec1 (sialoadhesin), 1054, 1080, 1081f,   eosinophils and, 954, 956t
                     DNA methyltransferase inhibitors, 775   1082, 1083f                    in Erdheim-Chester disease, 1111
                     fetal hemoglobin-inducing agents,   Siglec-2. See CD33                 hemorrhage, 1987
                         774–775                      Siglec 8, 949                         history of, 6
                     gene therapy, 453                Siglec 10, 949                        in juvenile xanthogranuloma, 1112
                     hematopoietic cell transplantation,   Signaling lymphocyte activation molecule   in Langerhans cell histiocytosis,
                         362–363, 775                        (SLAM), 54                           1103–1104, 1103f, 1106
                     histone deacetylase inhibitors, 775  Signal transduction pathways, 247–253  in mycosis fungoides. See Mycosis
                     hydroxyurea, 774, 774t, 775f       apoptosis and, 208–209, 208f              fungoides (MF)
                     investigative, 776, 777t           BCR-ABL1 and, 1443–1444, 1444f      primary lymphomas, 1581, 1665
                     iron overload associated with, 776  coordination and crosstalk, 253    in Rosai-Dorfman disease, 1113
                     potential targets, 767t            downstream signals, 250–252, 251f   in systemic mastocytosis, 973–974, 974f
                     red cell exchange, 430t, 431–432   extinguishing signals in, 252–253   in Waldenström macroglobulinemia, 1791
                     transfusions, 776, 2371–2372       insulation, 252                     warfarin-related necrosis, 396, 2100, 2100f,
                  Sickle cell-Hb C disease, 762         metabolism and, 193–196, 194f, 195f       2223
                  Sickle cells (drepanocytes), 473f, 473t, 474f,   overview, 247           Skin examination, 7–8
                         475                            in platelets. See Platelets, signaling   Skp2, 217
                  Sickle cell thalassemia, 749               pathways                      Skull lesions, in Langerhans cell histiocytosis,
                  Sickle cell trait (hemoglobin AS), 762, 766  receptors, 247–250, 248f. See also specific   1104, 1106
                  Side-population cells, 450                 receptors                     SLAM (signaling lymphocyte activation
                  Sideroachrestic anemia, 1342          specificity within receptor families, 252  molecule), 54
                  Sideroblastic anemias, 915–920      Silent alleles, blood group, 2339    SLC1A5 (ASCT2), 197, 198
                    classification, 916t              Silent β-thalassemia, 733, 750       SLC2A1 (GLUT1), 192
                    clinical and laboratory features, 920  Siltuximab                      SLC4A1, 664
                    definition and history, 915         for Castleman disease, 1250        SLC11A1 (Nramp1), 621, 1010, 1014
                    differential diagnosis, 637         for myeloma, 345f, 346t            SLC11A3. See Ferroportin (SLC40A1,
                    drugs causing, 916t, 919          Single-molecule sequencing, 158–159, 158f   SLC11A3)
                    epidemiology, 915                 Single nucleotide polymorphism (SNP), 147,   SLC19A2, 652
                    hereditary                               174                           SLC25A38, 916
                     autosomal, 890–891               Singlet oxygen, 284t, 286            SLC40A1. See Ferroportin (SLC40A1,
                     Pearson marrow-pancreas syndrome,   Sinus histiocytosis with massive         SLC11A3)
                         919, 920                            lymphadenopathy (Rosai-Dorfman   SLE. See Systemic lupus erythematosus (SLE)
                     X-linked, 894, 916–917, 920             disease), 1101, 1112–1113     SM (Sec1/Munc18), 1849
                     X-linked with ataxia, 918        Sinusoidal obstructive syndrome (SOS), 368  SMAC, 204f, 208, 1186
                    mitochondrial myopathy and, 919   SIN (self-inactivating) viral vectors, 437  SMAD, 251, 1713
                    pathogenesis                      siRNA, 153                           SMAD4, 621t
                     anemia mechanism, 919            Sirolimus                            SMAD anchor for receptor activation
                     heme synthesis defects, 916        for APECED syndrome, 1224                 (SARA), 251
                     metabolic defects, 918             in drug-eluting stents, 2297       Small G proteins, 1882–1883
                     mitochondrial myopathy, 919        for Erdheim-Chester disease, 1111  Small immature monocyte, 1045
                     morphology, 915–916, 916f          for IPEX syndrome, 1223            Small lymphocytic lymphoma (SLL), 184t,
                     pyridoxine metabolism, 917–918   Site I, 248                                 1533, 1592–1593, 1592f
                     ring sideroblast formation, 918  Site II, 248                         Small noncleaved cell (non-Burkitt)
                    primary acquired (clonal), 918–919  Sitosterolemia, 1996                      lymphoma, 187
                    secondary acquired, 919–920       Sjögren syndrome                     Small ubiquitin-like modifier (SUMO), 253
                    treatment, 920                      lymphocytopenia in, 1206           SMARCAL1, 1226
                  Sideroblasts                          lymphomas and, 1574–1575, 1664     SMC1A, 1346t, 1352
                    absence of, 552                     neutropenia in, 996                SMC3, 1346t, 1352








          Kaushansky_index_p2393-2506.indd   2491                                                                       9/21/15   3:22 PM
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